BRPI0606930A2 - compound or a pharmaceutically acceptable salt thereof, process for preparing a compound or a pharmaceutically acceptable salt thereof, pharmaceutical composition, use of a compound or a pharmaceutically acceptable salt thereof, and methods for producing a drug inhibiting effect. b-raf in a warm-blooded animal, for producing an anti-cancer effect on a warm-blooded animal and for treating diseases of an animal in a warm-blooded animal - Google Patents

compound or a pharmaceutically acceptable salt thereof, process for preparing a compound or a pharmaceutically acceptable salt thereof, pharmaceutical composition, use of a compound or a pharmaceutically acceptable salt thereof, and methods for producing a drug inhibiting effect. b-raf in a warm-blooded animal, for producing an anti-cancer effect on a warm-blooded animal and for treating diseases of an animal in a warm-blooded animal

Info

Publication number
BRPI0606930A2
BRPI0606930A2 BRPI0606930-4A BRPI0606930A BRPI0606930A2 BR PI0606930 A2 BRPI0606930 A2 BR PI0606930A2 BR PI0606930 A BRPI0606930 A BR PI0606930A BR PI0606930 A2 BRPI0606930 A2 BR PI0606930A2
Authority
BR
Brazil
Prior art keywords
pharmaceutically acceptable
acceptable salt
warm
compound
blooded animal
Prior art date
Application number
BRPI0606930-4A
Other languages
Portuguese (pt)
Inventor
Brian Aquila
Paul Lyne
Timothy Pontz
Original Assignee
Astrazeneca Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of BRPI0606930A2 publication Critical patent/BRPI0606930A2/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/42—One nitrogen atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

COMPOSTO OU UM SAL FARMACEUTICAMENTE ACEITáVEL DO MESMO, PROCESSO PARA PREPARAR UM COMPOSTO OU UM SAL FARMACEUTICAMENTE ACEITáVEL DO MESMO, COMPOSIçãO FARMACêUTICA, USO DE UM COMPOSTO OU DE UM SAL FARMACEUTICAMENTE ACEITáVEL DO MESMO, E, METODOS PARA A PRODUçãO DE UM EFEITO DE INIBIçãO DE B-RAF EM UM ANIMAL DE SANGUE QUENTE, PARA A PRODUçãO DE UM EFEITO ANTI-CáNCER EM UM ANIMAL DE SANGUE QUENTE E PARA O TRATAMENTO DE DOENçAS EM UM ANIMAL DE SANGUE QUENTE. A invenção refere-se a compostos químicos, ou a sais farmaceuticamente aceitáveis dos mesmos, da fórmula (1): que possuem atividade inbidora de B-Raf, úteis devido à sua atividade anti-câncer e, deste modo, em métodos de tratamento do corpo humano ou animal. A invenção também se refere à manufatura dos referidos químicos, a composições farmacêuticas contendo os mesmos e a compostos seu uso na manufatura de medicamentos para o uso na produção de um efeito anti-câncer em um animal de sangue quente, tal como o homem.COMPOSITE OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, PROCESS TO PREPARE PHARMACEUTICALLY ACCEPTABLE SALT OR PHARMACEUTICALLY COMPOSITION, USE OF A COMPOUND OR PHARMACEUTICALLY ACCEPTED SALT OF THESE AND METHOD B-RAF IN A HOT BLOOD ANIMAL, FOR THE PRODUCTION OF ANTI-CANCER EFFECT ON A HOT BLOOD ANIMAL AND FOR TREATMENT OF DISEASES IN A HOT BLOOD ANIMAL. The invention relates to chemical compounds, or pharmaceutically acceptable salts thereof, of formula (1): which have B-Raf inhibitory activity, useful because of their anti-cancer activity and, therefore, in methods of treatment of B-Raf. human or animal body. The invention also relates to the manufacture of said chemicals, pharmaceutical compositions containing them and compounds for use in the manufacture of medicaments for use in producing an anti-cancer effect in a warm-blooded animal such as man.

BRPI0606930-4A 2005-01-25 2006-01-24 compound or a pharmaceutically acceptable salt thereof, process for preparing a compound or a pharmaceutically acceptable salt thereof, pharmaceutical composition, use of a compound or a pharmaceutically acceptable salt thereof, and methods for producing a drug inhibiting effect. b-raf in a warm-blooded animal, for producing an anti-cancer effect on a warm-blooded animal and for treating diseases of an animal in a warm-blooded animal BRPI0606930A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US64682005P 2005-01-25 2005-01-25
PCT/GB2006/000223 WO2006079791A1 (en) 2005-01-25 2006-01-24 Chemical compounds

Publications (1)

Publication Number Publication Date
BRPI0606930A2 true BRPI0606930A2 (en) 2009-12-01

Family

ID=36588681

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0606930-4A BRPI0606930A2 (en) 2005-01-25 2006-01-24 compound or a pharmaceutically acceptable salt thereof, process for preparing a compound or a pharmaceutically acceptable salt thereof, pharmaceutical composition, use of a compound or a pharmaceutically acceptable salt thereof, and methods for producing a drug inhibiting effect. b-raf in a warm-blooded animal, for producing an anti-cancer effect on a warm-blooded animal and for treating diseases of an animal in a warm-blooded animal

Country Status (13)

Country Link
US (1) US20080146570A1 (en)
EP (1) EP1924573A1 (en)
JP (1) JP2008528473A (en)
KR (1) KR20070107061A (en)
CN (1) CN101146789A (en)
AU (1) AU2006208834A1 (en)
BR (1) BRPI0606930A2 (en)
CA (1) CA2594708A1 (en)
IL (1) IL184673A0 (en)
MX (1) MX2007008924A (en)
NO (1) NO20073719L (en)
WO (1) WO2006079791A1 (en)
ZA (1) ZA200706497B (en)

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JP2011513332A (en) * 2008-02-29 2011-04-28 アレイ バイオファーマ、インコーポレイテッド N- (6-Aminopyridin-3-yl) -3- (sulfonamido) benzamide derivatives as RAF inhibitors for the treatment of cancer
KR20100117686A (en) * 2008-02-29 2010-11-03 어레이 바이오파마 인크. Pyrazole [3,4-b] pyridine raf inhibitors
CA2716947A1 (en) * 2008-02-29 2009-09-11 Array Biopharma Inc. Imidazo [4,5-b] pyridine derivatives used as raf inhibitors
EP2265608A2 (en) * 2008-02-29 2010-12-29 Array Biopharma, Inc. Raf inhibitor compounds and methods of use thereof
US20120121515A1 (en) 2009-03-13 2012-05-17 Lenny Dang Methods and compositions for cell-proliferation-related disorders
CA2760911A1 (en) * 2009-05-19 2010-11-25 George E. Davis Compounds and methods for controlling fungi
ES2632954T3 (en) 2009-06-29 2017-09-18 Agios Pharmaceuticals, Inc. Quinoline-8-sulfonamide derivatives that have an anticancer activity
WO2011008788A1 (en) * 2009-07-14 2011-01-20 Dawei Zhang Fluoro-substituted compounds as kinase inhibitors and methods of use thereof
WO2011050210A1 (en) 2009-10-21 2011-04-28 Agios Pharmaceuticals, Inc. Methods and compositions for cell-proliferation-related disorders
US20140323519A1 (en) * 2011-04-26 2014-10-30 Merck Sharp & Dohme Corp. Heterocyclic compounds as b-raf inhibitors for treatment of cancer
SG194697A1 (en) 2011-05-03 2013-12-30 Agios Pharmaceuticals Inc Pyruvate kinase activators for use in therapy
CN102827073A (en) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 Therapeutically active compositions and application methods thereof
CN102827170A (en) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 Active treatment compositions and use method thereof
CN115536635A (en) 2012-01-06 2022-12-30 法国施维雅药厂 Therapeutically active compounds and methods of use thereof
WO2013109142A1 (en) 2012-01-16 2013-07-25 Stichting Het Nederlands Kanker Instituut Combined pdk and mapk/erk pathway inhibition in neoplasia
US9474779B2 (en) 2012-01-19 2016-10-25 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
CN102887860B (en) * 2012-09-29 2015-07-01 上海泰坦科技有限公司 Preparation method of 4-chloro-6-trifluoromethylpyrimidine type compound
EP2906212A4 (en) 2012-10-15 2016-06-08 Agios Pharmaceuticals Inc Therapeutic compounds and compositions
WO2015003355A2 (en) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
WO2015003360A2 (en) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
CN105492435B (en) 2013-07-11 2018-06-29 安吉奥斯医药品有限公司 Compound as IDH2 mutant inhibitor
US9579324B2 (en) 2013-07-11 2017-02-28 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
EP3019480B1 (en) 2013-07-11 2020-05-06 Agios Pharmaceuticals, Inc. 2,4- or 4,6-diaminopyrimidine compounds as idh2 mutants inhibitors for the treatment of cancer
US20150031627A1 (en) 2013-07-25 2015-01-29 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
WO2015041533A1 (en) 2013-09-20 2015-03-26 Stichting Het Nederlands Kanker Instituut Rock in combination with mapk-pathway
WO2015041534A1 (en) 2013-09-20 2015-03-26 Stichting Het Nederlands Kanker Instituut P90rsk in combination with raf/erk/mek
KR20240010105A (en) 2014-03-14 2024-01-23 아지오스 파마슈티컬스 아이엔씨. Pharmaceutical compositions of therapeutically active compounds
US11234976B2 (en) 2015-06-11 2022-02-01 Agios Pharmaceuticals, Inc. Methods of using pyruvate kinase activators
US10653710B2 (en) 2015-10-15 2020-05-19 Agios Pharmaceuticals, Inc. Combination therapy for treating malignancies
CA3216701A1 (en) 2015-10-15 2017-04-20 Les Laboratoires Servier Combination therapy for treating malignancies
US10980788B2 (en) 2018-06-08 2021-04-20 Agios Pharmaceuticals, Inc. Therapy for treating malignancies
US20220143049A1 (en) 2019-03-21 2022-05-12 Onxeo A dbait molecule in combination with kinase inhibitor for the treatment of cancer
JP2023500906A (en) 2019-11-08 2023-01-11 インサーム（インスティテュ ナシオナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシェ メディカル） Methods of treating cancers with acquired resistance to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
WO2023085142A1 (en) * 2021-11-12 2023-05-19 ユニマテック株式会社 Fluorine-containing pyrimidine compounds, harmful fungi control agent, and method for producing fluorine-containing pyrimidine compounds

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Also Published As

Publication number Publication date
MX2007008924A (en) 2007-08-21
WO2006079791A1 (en) 2006-08-03
KR20070107061A (en) 2007-11-06
AU2006208834A1 (en) 2006-08-03
IL184673A0 (en) 2007-12-03
ZA200706497B (en) 2008-08-27
CN101146789A (en) 2008-03-19
CA2594708A1 (en) 2006-08-03
JP2008528473A (en) 2008-07-31
US20080146570A1 (en) 2008-06-19
EP1924573A1 (en) 2008-05-28
NO20073719L (en) 2007-08-22

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B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

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B08H Application fees: decision cancelled [chapter 8.8 patent gazette]

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B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

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